Abstract

MicroRNAs (miRNAs) interfere with the translation of specific target mRNAs and are thought to thereby regulate many cellular processes. However, the role of miRNAs in osteoblast mechanotransduction remains to be defined. In this study, we investigated the ability of a miRNA to respond to different mechanical environments and regulate mechano-induced osteoblast differentiation. First, we demonstrated that miR-33-5p expressed by osteoblasts is sensitive to multiple mechanical environments, microgravity and fluid shear stress. We then confirmed the ability of miR-33-5p to promote osteoblast differentiation. Microgravity or fluid shear stress influences osteoblast differentiation partially via miR-33-5p. Through bioinformatics analysis and a luciferase assay, we subsequently confirmed that Hmga2 is a target gene of miR-33-5p that negatively regulates osteoblast differentiation. Moreover, miR-33-5p regulates osteoblast differentiation partially via Hmga2. In summary, our findings demonstrate that miR-33-5p is a novel mechano-sensitive miRNA that can promote osteoblast differentiation and participate in the regulation of differentiation induced by changes in the mechanical environment, suggesting this miRNA as a potential target for the treatment of pathological bone loss.

Highlights

  • Osteoblastogenesis and increased adipogenesis in human mesenchymal stem cells via the disruption of stress fibers, altered integrin signaling and down-regulated expression of well-known markers and regulators of osteoblast differentiation, including osteocalcin (OC), type I collagen α 1 (Col-Iα 1), dentin matrix protein 1 (DMP1) and runt-related transcription factor 2 (Runx2)[15,16]

  • Results miR-33-5p levels in MC3T3-E1 cells are altered under different mechanical environments

  • A recent study demonstrated that miRNAs respond to mechanical loading and play essential roles in osteoblast differentiation and bone formation[28]

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Summary

Introduction

Osteoblastogenesis and increased adipogenesis in human mesenchymal stem cells (hMSC) via the disruption of stress fibers, altered integrin signaling and down-regulated expression of well-known markers and regulators of osteoblast differentiation, including osteocalcin (OC), type I collagen α 1 (Col-Iα 1), dentin matrix protein 1 (DMP1) and runt-related transcription factor 2 (Runx2)[15,16]. MicroRNAs (miRNAs) are endogenously expressed non-coding single-stranded RNAs of 20–24 nucleotides that post-transcriptionally regulate gene expression. Their regulatory functions are widespread in various biological processes[17,18]. MiR-210 ameliorates postmenopausal osteoporosis due to estrogen deficiency by promoting VEGF expression and osteoblast differentiation[21] These findings demonstrate that miRNAs significantly impact osteoblast differentiation. MiR-153 is sensitive to mechanical loading and regulates osteoblast differentiation by directly targeting BMPR224. These results demonstrate that miRNAs may play a critical role in the sensing of mechanical loads by osteoblasts. This study may provide a novel mechanism and potential therapeutic target for skeletal disorders caused by pathological mechanical environments

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